List of variants in gene MLYCD reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_012213.3(MLYCD):c.528+118T>G	rs185230073	0.00530
NM_012213.3(MLYCD):c.949-149A>G	rs114202583	0.00510
NM_012213.3(MLYCD):c.206C>T (p.Ala69Val)	rs200579941	0.00284
NM_012213.3(MLYCD):c.1044G>T (p.Glu348Asp)	rs138675420	0.00118
NM_012213.3(MLYCD):c.408C>G (p.Arg136=)	rs183593320	0.00108
NM_012213.3(MLYCD):c.375C>G (p.Ala125=)	rs375657338	0.00096
NM_012213.3(MLYCD):c.1007A>G (p.Lys336Arg)	rs76841036	0.00075
NM_012213.3(MLYCD):c.1098C>T (p.Ile366=)	rs199549095	0.00048
NM_012213.3(MLYCD):c.1074G>A (p.Ser358=)	rs377161125	0.00043
NM_012213.3(MLYCD):c.1383G>A (p.Thr461=)	rs375344095	0.00027
NM_012213.3(MLYCD):c.393C>T (p.Tyr131=)	rs560831102	0.00015
NM_012213.3(MLYCD):c.1146C>T (p.Ser382=)	rs373273203	0.00010
NM_012213.3(MLYCD):c.1191G>A (p.Pro397=)	rs753701525	0.00001
NC_000016.10:g.83898796C>A	rs145585258
NM_012213.3(MLYCD):c.529-20A>G	rs1555538216
NM_012213.3(MLYCD):c.798+107del	rs558316423

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.